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TPIDB > Principal Investigator

Principal Investigator



更新時間:2024-06-04

鐘育志Jong, Yuh-Jyh
  • Principal Investigator
  • Clinical Trial Experience (year) 17 years 9 個月
  • wendychoucrn@gmail.com

  • wendychoucrn@gmail.com

篩選

List

25Cases

2013-08-01 - 2016-11-30

Phase III

Completed
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial of Tadalafil for Duchenne Muscular Dystrophy
  • Condition/Disease

    Duchenne Muscular Dystrophy

  • Test Drug

    Tadalafil (LY450190)

Participate Sites
2Sites

Terminated2Sites

2021-11-01 - 2026-02-09

Phase III

Completed
A Randomized, Sham-controlled, Double-blind Study to Evaluate the Efficacy and Safety of Intrathecal OAV101 in Type 2 Spinal Muscular Atrophy (SMA) Patients Who Are ≥ 2 to < 18 Years of Age, Treatment Naive, Sitting, and Never Ambulatory
  • Condition/Disease

    Patients aged 2 to under 18 years with treatment-naïve, late-onset type 2 spinal muscular atrophy (SMA) who are able to sit but have never walked.

  • Test Drug

    OAV101

Participate Sites
2Sites

Not yet recruiting1Sites

Study ended1Sites

2021-09-30 - 2023-08-01

Phase III

Completed
A Phase IIIb, open-label, single-arm, single-dose, multicenter study to evaluate the safety, tolerability and efficacy of gene replacement therapy with intravenous OAV101 (AVXS-101) in pediatric patients with spinal muscular atrophy (SMA)
  • Condition/Disease

    Pediatric patients with spinal muscular atrophy (SMA)

  • Test Drug

    OAV101

Participate Sites
2Sites

Recruiting1Sites

Study ended1Sites

2023-01-10 - 2031-02-26

Phase IV

Active
  • Condition/Disease

  • Test Drug

Participate Sites
2Sites

Recruiting2Sites

2024-04-01 - 2030-11-15

Phase III

Active
  • Condition/Disease

  • Test Drug

Participate Sites
2Sites

Not yet recruiting2Sites

2021-03-17 - 2035-12-31

Others

  • Condition/Disease

  • Test Drug

Participate Sites
5Sites

Not yet recruiting2Sites

Recruiting3Sites

2015-10-28 - 2015-10-28

Phase III

An Open-label Extension Study of the Long-term Safety, Tolerability and Efficacy of Drisapersen in Subjects With Duchenne Muscular Dystrophy.
  • Condition/Disease

    Duchenne muscular dystrophy

  • Test Drug

    drisapersen

Participate Sites
1Sites

Terminated1Sites

2010-11-24 - 2010-11-24

Phase III

  • Condition/Disease

  • Test Drug

Participate Sites
1Sites

Terminated1Sites

2017-09-01 - 2021-12-31

Phase III

A Phase 3, Randomized, Double-blind, Placebo-controlled Efficacy and Safety Study of Ataluren in Patients With Nonsense Mutation Duchenne Muscular Dystrophy and Open-Label Extension
  • Condition/Disease

    Genetic Disorders – Duchenne Muscular Dystrophy

  • Test Drug

    Ataluren (PTC124)

Participate Sites
2Sites

Recruiting2Sites

1 2 3